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临床试验/NCT06905418
NCT06905418进行中(未招募)不适用

Design and Validation of a Mobile Health Application for Home-Based Musculoskeletal Therapy in Ankle Sprain

Superior University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年3月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
100
试验地点
1
主要终点
Foot and Ankle Ability Measure (FAAM)

研究概览

简要总结

"Ankle sprain is a common musculoskeletal injury that can pointedly influence the quality of life of an indivual. Old rehabilitation approaches often require recurrent clinic visits, which can be time-consuming, costly, and unreachable to many. This study aims to design and validate a mobile health application for home-based musculoskeletal therapy in ankle sprain.

详细描述

The study will employ a randomized controlled trial design, involving patients with ankle sprains, healthcare professionals, and healthy volunteers. The mobile health application will be designed to provide personalized exercises, education, and monitoring to improve rehabilitation outcomes. The study will evaluate the effects of the mobile health application (m Health) in reducing pain, improving functional ability, and ornamental quality of life. The study will also assess the usability and acceptability of the application among patients and healthcare professionals.

Outcome measurement tools will contain the Foot and Ankle Ability Measure (FAAM), Numeric Pain Rating Scale (NPRS) and System Usability Scale (SUS) The study will contribute to the development of an innovative, home-based rehabilitation solution for individuals with ankle sprains, improving accessibility and adherence to rehabilitation programs.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults, 18-65 years, both gender(male and female) will be included.
  • •Include participants clinically diagnosed with a lateral ankle sprain confirmed by a healthcare professional, with a clear timeframe such as within the last 4-6 weeks.
  • •Grade I and II sprains (mild to moderate) will be included using NPRS tool range from 0 to
  • •Participants must own and be able to use a smartphone or tablet that is compatible with the mobile health application.
  • •Specify that participants must be able to read and understand the application interface language.
  • •Ensure participants can safely perform the exercises prescribed in the app without additional risk of injury

排除标准

  • •Concurrent fractures of the leg or foot.
  • •Previous surgery in the affected ankle or surgery resulting from the current ankle sprain.
  • •Serious systemic illnesses (e.g. rheumatoid arthritis, or fibromyalgia).
  • •Neurological impairments or other conditions that may affect rehabilitation outcomes

研究组 & 干预措施

Clinic

Experimental

干预措施: Clinic (Diagnostic Test)

Mobile App

Experimental

干预措施: Mobile App (Combination Product)

结局指标

主要结局

Foot and Ankle Ability Measure (FAAM)

时间窗: 12 Months

FAAM. Each item of the FAAM is scored on a 5-point Likert scale with 4 points representing no difficulty at all; 3 points, slight difficulty; 2 points, moderate difficulty; 1 point, extreme difficulty; and 0 points, unable to do

Numeric pain rating scale (NPRS)

时间窗: 12 months

The Numeric Pain Rating Scale (NPRS) is perhaps the most frequently applied scale used to quantify pain intensity in the clinical setting. It is an 11-point numeric scale, ranging from 0 indicating no pain to 10 indicating worst pain imaginable

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Muhammad Naveed Babur

Principal Investigator

Superior University

研究点 (1)

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